WormBase Tree Display for DO_term: DOID:0060485
expand all nodes | collapse all nodes | view schema
| DOID:0060485 | Name | Mowat-Wilson syndrome | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | A syndrome characterized by distinctive facial features, intellectual disability, delayed development, Hirschsprung disease and has_material_basis_in de novo heterozygous mutation in the ZEB2 gene on chromosome 2q22. | ||||
| Synonym | Exact (2) | ||||
| Parent | Is_a (2) | ||||
| DB_info | Database | OMIM | disease | 235730 | |
| Attribute_of | Gene_by_orthology | WBGene00006970 |
